Hyphen Biomed

Hyphen Biomed — FDA 510(k) Submissions

Hyphen Biomed has submitted 6 FDA 510(k) premarket notifications since 2005, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plasma, Coagulation Control, Antithrombin Iii Quantitation, Test, Qualitative And Quantitative Factor Deficiency, Assay, Heparin, Platelet Factor 4 Radioimmunoassay . Use the specialty filter in the sidebar to narrow results.